Evidence map›Paper›PMID 31801090›Full record

ArticleCell reports2019

Discovery of Small Molecules for the Reversal of T Cell Exhaustion.

Brett S Marro, Jaroslav Zak, Reza Beheshti Zavareh, John R Teijaro, Luke L Lairson, Michael B A Oldstone

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.1field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 47 citations in OpenAlex.

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  18. Immune Checkpoint Receptors Signaling in T Cells.International journal of molecular sciences · 2022
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Brett S MarroDepartment of Immunology and Microbial Science, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Jaroslav ZakDepartment of Immunology and Microbial Science, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Reza Beheshti ZavarehDepartment of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
John R TeijaroDepartment of Immunology and Microbial Science, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Luke L LairsonDepartment of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Michael B A OldstoneDepartment of Immunology and Microbial Science, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA. Electronic address: mbaobo@scripps.edu.
Scripps Research Institute · US

Funding

PATHOGENESIS OF PERSISTENT VIRAL INFECTIONR01AI009484 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI OLDSTONE, MICHAEL B · 1985 to 2016
$7.2M
IL-27 elicited antibodies: A novel means to control persistent Arenavirus infectionR01AI118862 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI TEIJARO, JOHN ROSS · 2016 to 2020
$2.4M
Novel Strategies for Controlling Persistent Viral InfectionR01AI123210 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI TEIJARO, JOHN ROSS · 2016 to 2019
$1.9M
Host Genetic Factors to Combat Lassa Hemorrhagic FeverR01AI099699 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI OLDSTONE, MICHAEL B · 2013 to 2016
$1.9M
Pathogenesis and Novel Therapeutics to Reverse T Cell Exhaustion in Persistent Viral InfectionsR21AI141842 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI LAIRSON, LUKE LEE · 2019 to 2020
$532k
NIAID NIH HHS R01 AI009484NIAID NIH HHS R01 AI099699NIAID NIH HHS R01 AI118862NIAID NIH HHS R01 AI123210NIAID NIH HHS R21 AI141842
6 · The paper itself

Abstract

Inhibitory receptors (IRs) function as critical regulators of immune responses by tempering T cell activity. In humans, several persisting viruses as well as cancers exploit IR signaling by upregulating IR ligands, resulting in suppression of T cell function (i.e., exhaustion). This allows escape from immune surveillance and continuation of disease. Here, we report the design, implementation, and results of a phenotypic high-throughput screen for molecules that modulate CD8

Indexed as

AnimalsCD8-Positive T-LymphocytesCell ProliferationChlorocebus aethiopsCostimulatory and Inhibitory T-Cell ReceptorsCytokinesImmunotherapyMaleMiceMice, Inbred C57BLProtein Kinase CSignal TransductionSmall Molecule LibrariesVero CellsCostimulatory and Inhibitory T-Cell ReceptorsCytokinesProtein Kinase CSmall Molecule LibrariesCD8 T cellcheckpoint blockadechronic infectionhigh-throughput flow cytometryingenol mebutatePKCT cell exhaustion

Identifiers

PMID31801090
PMCPMC6931400
OpenAlexW2993746034

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.